GB1191615A - Anthraquinone Dyestuffs - Google Patents

Anthraquinone Dyestuffs

Info

Publication number
GB1191615A
GB1191615A GB359069A GB359069A GB1191615A GB 1191615 A GB1191615 A GB 1191615A GB 359069 A GB359069 A GB 359069A GB 359069 A GB359069 A GB 359069A GB 1191615 A GB1191615 A GB 1191615A
Authority
GB
United Kingdom
Prior art keywords
alkyl
aryl
anthraquinone
compound
condensing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB359069A
Inventor
Heinz Machatzke
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer AG
Original Assignee
Bayer AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bayer AG filed Critical Bayer AG
Publication of GB1191615A publication Critical patent/GB1191615A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/56Mercapto-anthraquinones
    • C09B1/58Mercapto-anthraquinones with mercapto groups substituted by aliphatic, cycloaliphatic, araliphatic or aryl radicals
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/02Hydroxy-anthraquinones; Ethers or esters thereof
    • C09B1/06Preparation from starting materials already containing the anthracene nucleus
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16Amino-anthraquinones
    • C09B1/20Preparation from starting materials already containing the anthracene nucleus
    • C09B1/202Preparation from starting materials already containing the anthracene nucleus sulfonated
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/52Amino-hydroxy-anthraquinones; Ethers and esters thereof sulfonated
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/54Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
    • C09B1/545Anthraquinones with aliphatic, cycloaliphatic or araliphatic ether groups
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/54Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
    • C09B1/547Anthraquinones with aromatic ether groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1,191,615. Anthraquinone dyestuffs. FARBENFABBIKEN BAYER A.G. 22 Jan., 1969 [27 Jan., 1968], No. 3590/69. Heading C4P. The invention comprises anthraquinone dyestuffs of the general formula wherein A is -CH 2 -, -CH-(alkyl), -CO-, or -SO 2 -, Z is a saturated or unsaturated optionally substituted C 2 -C 12 alkylene radical or a condensed optionally hydrogenated arylene radical of the benzene or naphthalene series, Y is a direct bond or a divalent bridge member; R 1 to R 5 independently are each H, halogen (Cl, Br, F), -NO 2 , -NH 2 , -NHalkyl, -NH- aryl, -NH-acyl, -O- alkyl, -O-aryl, -OH, -S-alkyl, -S-aryl, -SO 2 NH-alkyl, -SO 2 N(alkyl) 2 , -SO 2 NH-aryl, -SO 2 -alkyl, -SO 2 -aryl or -aryl, and R 1 may also be C 1 -C 4 alkyl or a carboxy group, the radicals X are sulphonic acid groups, p and p<SP>1</SP> are 1, 2 or 3, m is 0, 1 or 2, and n is 0, 1 or 2, the sum m + n being at least 1. They are prepared by (a) sulphonating a corresponding dyestuff which is completely free of sulphonic acid groups or is sulphonated in the anthraquinone nucleus preferably using 2 to 65% oleum at 0‹ to 150‹ C.; (b) condensing a compound having a group -Y-phenyl in the 2-position with a cyclic N- methylol amide, or a derivative thereof which reacts in the same manner preferably in presence of 80-100% sulphuric, 80-100% phosphoric or a mixture of acetic and hydrochloric acids; or (c) condensing an anthraquinone compound having a replaceable substituent V in the 2-position with a compound of the formula wherein R 1 , p, X, m, A, Y and Z are as defined in Claim 1 with elimination of VH. The dyes give orange, red, blue, violet and grey shades on wool and synthetic polyamides.
GB359069A 1968-01-27 1969-01-22 Anthraquinone Dyestuffs Expired GB1191615A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19681644624 DE1644624A1 (en) 1968-01-27 1968-01-27 Anthraquinone dyes
DEF0054658 1968-01-27

Publications (1)

Publication Number Publication Date
GB1191615A true GB1191615A (en) 1970-05-13

Family

ID=25754097

Family Applications (1)

Application Number Title Priority Date Filing Date
GB359069A Expired GB1191615A (en) 1968-01-27 1969-01-22 Anthraquinone Dyestuffs

Country Status (6)

Country Link
BE (1) BE727390A (en)
CH (1) CH502411A (en)
DE (1) DE1644624A1 (en)
FR (1) FR1601914A (en)
GB (1) GB1191615A (en)
NL (1) NL6900969A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3758505A (en) * 1971-04-16 1973-09-11 Gaf Corp Anthraquinone dyes containing n methylenelactam
DE59108142D1 (en) * 1990-12-06 1996-10-10 Hoechst Ag Pigment preparations

Also Published As

Publication number Publication date
FR1601914A (en) 1970-09-21
CH502411A (en) 1971-01-31
DE1644624A1 (en) 1971-05-13
NL6900969A (en) 1969-07-29
BE727390A (en) 1969-07-01

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Legal Events

Date Code Title Description
PS Patent sealed
PLNP Patent lapsed through nonpayment of renewal fees